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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928536Generated: October 31, 2026

4-Toluenesulfonyl chloride → N-Boc-4-[2-(4-Toluenesulfonyloxy)ethyl]piperidine

https://huagongshe.com/reaction/1928536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
SolventDichloromethaneHCID 6344—
ProductN-Boc-4-[2-(4-Toluenesulfonyloxy)ethyl]piperidineHCID 2193607089.4%

Reaction Steps

To an ice-cold solution of N-Boc-4-piperidine-ethanol (5.0 g, 21.8 mmol) and Et3N (4.6 mL, 33.0 mmol) in dry DCM (10 mL) was added p-toluenesulfonyl chloride (6.25 g, 32.8 mmol) slowly. Upon addition, the reaction was warmed to room temperature and stirred for 20 h. The reaction mixture was washed with water (40 mL), 10% (wt/v) citric acid(aq) (40 mL), and saturated NaHCO3(aq) (40 mL). The DCM layer was dried with MgSO4, filtered and concentrated in vacuo to give a pale yellow oil, which was chromatographed to give the title compound (7.47 g, 89% yield) as a clear and colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183374B2
Source datasetuspto-grants-2012_05
ORD IDord-ca5c116d8d964259a7ff23246477fc7b
Source noteuspto-grants-2012_05